raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:716422

Rare disorder with non-progressive predominantly macular disorder as a major feature

Synonyms: Rare syndromic non-progressive predominantly macular disorder

Type
Category
Group
Group of disorders
Status
active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

1

Names in Orphadata languages

9 of 12 languages
LangNameSynonyms
enRare disorder with non-progressive predominantly macular disorder as a major featureRare syndromic non-progressive predominantly macular disorder
frMaladie rare avec atteinte non-progressive prédominante de la macula comme manifestation majeure rareMaladie rare avec atteinte non-progressive prédominante de la macula syndromique
deSeltene Störung mit nicht-progredienter Makulopathie als Hauptmerkmal
esTrastorno raro con afectación predominantemente macular no progresiva como característica principalTrastorno raro predominantemente macular no progresivo sindrómico
itMalattia rara con predominante maculopatia non progressiva come caratteristica principaleMalattia rara sindromica non progressiva a predominanza maculare
nlZeldzame aandoening met niet-progressieve overwegend maculaire aandoening als een hoofdkenmerkZeldzame syndromale niet-progressieve overwegend maculaire aandoening · Zeldzame syndromale niet-progressieve aandoening van voornamelijk macula · Zeldzame syndromale niet-progressieve aandoening van voornamelijk gele vlek
ptRare disorder with non-progressive predominantly macular disorder as a major feature
plRzadkie postępujące zaburzenie z zajęciem głównie plamki jako dominującą cechą= en
csRare disorder with non-progressive predominantly macular disorder as a major feature= en
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (2):

Children (1):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card